Английская Википедия:APH-1

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Версия от 04:15, 27 декабря 2023; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Short description|Protein gene product}} {{protein |Name=anterior pharynx defective 1 homolog A (C. elegans) |caption= |image= |width= |HGNCid=29509 |Symbol=APH1A |AltSymbols= |EntrezGene=51107 |OMIM=607629 |RefSeq=NM_016022 |UniProt=Q96BI3 |PDB= |ECnumber= |Chromosome=1 |Arm=p |Band=36.13 |LocusSupplementaryData=-q31.3 }} {{protein |Name=anterior pharynx defective 1 homolog B (C. el...»)
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Шаблон:Short description Шаблон:Protein Шаблон:Protein APH-1 (anterior pharynx-defective 1) is a protein gene product originally identified in the Notch signaling pathway in Caenorhabditis elegans as a regulator of the cell-surface localization of nicastrin.[1] APH-1 homologs in other organisms, including humans, have since been identified as components of the gamma secretase complex along with the catalytic subunit presenilin and the regulatory subunits nicastrin and PEN-2. The gamma-secretase complex is a multimeric protease responsible for the intramembrane proteolysis of transmembrane proteins such as the Notch protein and amyloid precursor protein (APP). Gamma-secretase cleavage of APP is one of two proteolytic steps required to generate the peptide known as amyloid beta, whose misfolded form is implicated in the causation of Alzheimer's disease.[2] All of the components of the gamma-secretase complex undergo extensive post-translational modification, especially proteolytic activation; APH-1 and PEN-2 are regarded as regulators of the maturation process of the catalytic component presenilin.[3] APH-1 contains a conserved alpha helix interaction motif glycine-X-X-X-glycine (GXXXG) that is essential to both assembly of the gamma secretase complex and to the maturation of the components.[4]

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Шаблон:Gene-15-stub